Epoxi-amine composition modified with hydroxyalkyl urethane

a technology of hydroxyalkyl urethane and epoxi-amine, which is applied in the field of epoxi-amine compositions, can solve the problems of limited influence of benzyl alcohol and acids as accelerators, inability to stabilize reactive adducts, and inability to cure epoxy polymers, so as to accelerate curing reaction, improve wear resistance and mechanical properties, and reduce chemical resistance

Active Publication Date: 2010-09-30
LIFSCHITZ YAKOV MARK +1
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  • Summary
  • Abstract
  • Description
  • Claims
  • Application Information

AI Technical Summary

Benefits of technology

[0029]Introduction of HUM accelerates the curing reaction and at the same time improves wear resistance and mechanical properties without decreasing chemical resistance of the final cured polymer product.

Problems solved by technology

The accelerators also act as plasticizers to the epoxy matrix and reduce the chemical resistance of the resulting cured epoxy polymer.
A particular problem exists with the use of phenol as an accelerator, since it is highly corrosive to skin and is coming under an increasing regulatory pressure.
Furthermore, the effect of phenol, nonyl phenol, benzyl alcohol and acids as accelerators are limited in their influence on a cure rate or physical and chemical properties of the resulting cured epoxy product.
However they are fugitive and can effect the environment.
These reactive adducts are not stable due to an aminolysis reaction that increases viscosity during storage.
The resulting polymer is too viscous and demands the use of organic solvents and increased temperatures.

Method used

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  • Epoxi-amine composition modified with hydroxyalkyl urethane
  • Epoxi-amine composition modified with hydroxyalkyl urethane
  • Epoxi-amine composition modified with hydroxyalkyl urethane

Examples

Experimental program
Comparison scheme
Effect test

examples

Synthesis of Hydroxyalkyl urethane Modifier HUM-1

[0083]15.8 g (0.2 AEW) of TMD and 20.4 g (0.2 CCEW) of PC, ratio 1:1, were put into a 100 ml flask and then the mixture was stirred. The reaction mixture was kept in the flask at room temperature during 6 hours and the consumption of the cyclic carbonate groups was controlled by spectrometer FT / IR, (wavelength 1800 cm−1).

[0084]Calculated molecular mass of HUM-1 was 362.

[0085]Solids content (60°, 110° C.) was 97%.

[0086]Viscosity (25° C.) was 79 Pa·s.

Synthesis of Hydroxyalkyl Urethane Modifier HUM-2

[0087]17.0 g (0.2 AEW) of IPDA and 22.4 g (0.22 CCEW) of PC, ratio 1:1.1, were loaded into a 100 ml flask, and then the mixture was stirred. The reaction mixture was kept in the flask at room temperature during 6 hours, and the consumption of the cyclic carbonate groups was controlled by spectrometer FT / IR, (wavelength 1800 cm−1).

[0088]Calculated molecular mass of HUM-2 was 374.

[0089]Solids content (60°, 110° C.) was 96%.

[0090]Viscosity (50° ...

example 1

Composition 1

[0105]18.7 g (0.1 EEW) of DER-331

[0106]0.9 g (5% to epoxy resin) HUM-1

[0107]The mixture was put into a 50 ml vessel, was stirred and heated at 50° C. for 30 min.

[0108]Then the mixture was cooled to RT, 4.0 g (0.1 AHEW) of TMD was added, and the mixture was repeatedly stirred for 2 minutes.

[0109]Then the mixture was poured into standard moulds.

Composition 2

[0110]18.7 g (0.1 EEW) of DER-331

[0111]1.9 g (10% to epoxy resin) HUM-1

[0112]The mixture was placed into a 50 ml vessel, was stirred and heated at 50° C. for 30 min. Then the mixture was cooled to RT, 4.0 g (0.1 AHEW) of TMD was added, and the mixture was repeatedly stirred for 2 minutes.

[0113]Then the mixture was loaded into standard moulds.

Composition 3

[0114]18.7 g (0.1 EEW) of DER-331

[0115]2.8 g (15% to epoxy resin) HUM-1

[0116]The mixture was placed into a 50 ml vessel, and stirred and heated at 50° C. for 30 min.

[0117]Then the mixture was cooled to RT, 4.0 g (0.1 AHEW) of TMD was added, and the mixture was repeated...

example 2

Preparation of epoxy-amine composition—ST-3000, TMD, HUM-2

[0140]Comparative Composition 2 was used in this EXAMPLE.

[0141]The mixture was put into a 50 ml vessel and was stirred for 2 minutes.

[0142]Then the mixture was poured into standard moulds.

Composition 6

[0143]22.5 g (0.1 EEW) ST-3000

[0144]1.1 g (5.0% to epoxy resin) HUM-2

[0145]The mixture was put into a 50 ml vessel, was stirred and heated at 50° C. during 30 min

[0146]Then the mixture was cooled to RT, 4.0 g (0.1 AHEW) of TMD was added, and the mixture was repeatedly stirred for 2 minutes.

[0147]Then the mixture was applied to standard moulds.

Composition 7

[0148]22.5 g (0.1 EEW) ST-3000

[0149]2.2 g (10% to epoxy resin) HUM-2

[0150]The mixture was put into a 50 ml vessel, was stirred and heated at 50° C. during 30 min.

[0151]Then the mixture was cooled to RT, 4.0 g (0.1 AHEW) of TMD was added, and the mixture was repeatedly stirred for 2 minutes.

[0152]Then the mixture was placed into standard moulds.

Composition 8

[0153]22.5 g (0.1 EEW...

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Abstract

Disclosed is a novel epoxy-amine composition modified a hydroxyalkyl urethane, which is obtained as a result of a reaction between a primary amine (C1) and a monocyclocarbonate (C2), wherein modifier (C) is represented by the following formula (1):
wherein R1 is a residue of the primary amine, R2 and R3 are the same or different and are selected from the group consisting of H, alkyl, hydroxyalkyl, and n satisfies the following condition: n≧2. Diluents, pigments and additives can be used. Doping with the hydroxyalkyl-urethane modifier imparts to the cured composition superior coating performance characteristics, such as pot-life/drying, strength-stress, bonding, appearance, resistance to abrasion and solvents, etc., in a well-balanced state.

Description

FIELD OF THE INVENTION[0001]This invention relates to epoxy-amine compositions, in particular to epoxy-amine compositions modified with hydroxyalkyl urethane. The compositions of the invention can be used for forming adhesives, sealants, and coatings having high resistance to wear.BACKGROUND OF THE INVENTION[0002]It is known that three-dimensional epoxy-amine networks produced by curing epoxy compositions that contain a liquid epoxy resin and amino hardeners normally exhibit desirable properties. Therefore, amine-curable epoxy resin systems find wide application in the industry as coatings, adhesives, sealants, or matrices for components. Some applications require increase in the reaction rate which is normally achieved by adding accelerators. Various accelerators, such as phenol compounds, benzyl alcohol, carboxylic acids etc., are currently used by the industry to accelerate the curing process with commonly used amines and amine adducts. As these accelerators migrate from the cure...

Claims

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Application Information

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Patent Type & Authority Applications(United States)
IPC IPC(8): C08G65/333
CPCC08G59/4014C08G59/56C08G65/33306C08G2650/50C08L71/02C08L63/00C08L2666/22
Inventor BIRUKOV, OLGAFIGOVSKY, OLEGLEYKIN, ALEXANDERSHAPOVALOV, LEONID
Owner LIFSCHITZ YAKOV MARK
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